Evidence map›Paper›PMID 42649337›Full record

ArticleJournal of imaging informatics in medicine2026

Deep Learning-Based Classification of NIFTP and Invasive Encapsulated Follicular Variant of Papillary Thyroid Carcinoma Using Gross Pathology Images.

Chung-Hsin Tsai, I-An Chien, Chi-Yu Kuo, Shih-Ping Cheng

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Article in Journal of imaging informatics in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chung-Hsin TsaiDepartment of Surgery, MacKay Memorial Hospital, 92, Chung-Shan North Road, Section 2, Taipei, 104217, Taiwan.
I-An ChienDepartment of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Chi-Yu KuoDepartment of Surgery, MacKay Memorial Hospital, 92, Chung-Shan North Road, Section 2, Taipei, 104217, Taiwan.
Shih-Ping ChengDepartment of Surgery, MacKay Memorial Hospital, 92, Chung-Shan North Road, Section 2, Taipei, 104217, Taiwan. surg.mmh@gmail.com.ORCID http://orcid.org/0000-0002-6301-5096

Funding

Mackay Memorial Hospital MMH-116-009Mackay Memorial Hospital MMH-E-115-08National Science and Technology Council NSTC-114-2314-B-195-014-MY3
6 · The paper itself

Abstract

Non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) and invasive encapsulated follicular variant of papillary thyroid carcinoma (IEFVPTC) are diagnostically challenging thyroid neoplasms with overlapping clinical and molecular characteristics. Although artificial intelligence has shown promise for diagnostic support in radiology and histopathology, its application to gross pathology remains unexplored. This study analyzed gross pathology photographs from 87 patients (43 with NIFTP and 44 with IEFVPTC). Three frozen, pretrained convolutional neural network backbones (EfficientNet, ResNet, and ConvNeXt) were used to generate feature embeddings, which were subsequently classified using Random Forest, support vector machine, and Gradient Boosting algorithms. Patient-level nested stratified five-fold cross-validation with inner hyperparameter tuning was used to generate unbiased out-of-fold predictions. EfficientNet combined with Random Forest was prespecified as the primary model and achieved a pooled area under the receiver operating characteristic curve (AUC) of 0.788 (95% CI, 0.614-0.928). Among the eight exploratory backbone-classifier combinations, pooled AUCs ranged from 0.500 to 0.755, and no pairwise comparison, including comparisons with the primary model, remained significantly different after Benjamini-Hochberg correction. The primary model demonstrated a sensitivity of 0.588, specificity of 0.944, accuracy of 0.771, and F1 score of 0.714. Gradient-weighted class activation mapping (Grad-CAM) revealed that all backbones predominantly highlighted lesional tissue rather than background regions, although activation patterns differed across architectures. In conclusion, this proof-of-concept study demonstrates that gross pathology images contain modest discriminative information for distinguishing NIFTP from IEFVPTC. These findings support the concept that macroscopic morphology encodes subtle yet class-separating signals.

Indexed as

Deep learningGross pathologyNIFTPThyroid neoplasms

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.